DDV LIGATOR— 510(k) K921304

Substantially Equivalent

North American Medical, Inc.

FDA 510(k) clearance K921304 for DDV LIGATOR, Substantially Equivalent on 1992-10-05. Applicant: North American Medical, Inc.. Device class: 1.

Clearance details

Applicant: North American Medical, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1992-03-11
Decision date: 1992-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lubbock, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.